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Clinical Trial Summary

Extension of the PFBIO cohort which includes patients with newly diagnosed idiopathic pulmonary fibrosis (IPF) for longitudinal follow-up for up to 5 years. In the PFBIO-EXA extension, patients are included if they experience an exacerbation, or other increase in respiratory symptoms requiring hospital admission, for further collection of clinical and biological data.


Clinical Trial Description

The aim of this study is to investigate the diagnostic and prognostic value of clinical and blood biomarkers during exacerbations, or other increase in respiratory symptoms requiring hospital admission in patients with IPF. Patients that are already included in the PFBIO-cohort (NCT02755441) and who are admitted to hospital with an increase in respiratory symptoms, are also included in PFBIO-EXA. Patients are recruited within 24 hrs. from hospital admission with respiratory worsening, where clinical data, and blood samples are collected. The blood samples are investigated for the same blood biomarkers as PFBIO. Patient related outcomes are also collected, including quality-of-life questionnaires and outcomes of the exacerbations. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04442711
Study type Observational
Source University Hospital, Gentofte, Copenhagen
Contact
Status Recruiting
Phase
Start date June 13, 2020
Completion date December 31, 2028

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